J. C. Ppppppp and A. H. Zzz, Accounts of Chemical Research, vol.28, issue.7, pp.119-132, 1995.

F. , J. Ppp, F. Tt, and M. , Journal of Organometallic Chemistry, vol.208, pp.419-427, 1981.

A. Bbbb, J. ;. Hhhhhh, A. Pppppp, G. Ppppp, and G. , Chemistry3 : Introducing Inorganic, Organic and Physical Chemistry, vol.27, p.24, 2017.

B. Ttttttt and G. Dddddd, Techniques de l'ingénieur Électrochimie, 2001.

A. , L. Vvvvvvv, R. Kkkkk, and A. R. , ) EEEEEEEEE, E. Nouvelles applications de la réaction de Passerini dans des réactions de type Friedel-Crafts et Tsuji-Trost., Ecole Polytechnique, vol.157, p.152, 2009.

B. M. Tt, D. L. Vvvvvvv, B. M. Tt, N. A. Bbbb, and W. Zzzz, DOI : 10.1021/ cr9409804, Chemical Society Reviews, vol.96, p.128, 1996.

J. ;. Ttttt, H. Mmmmmm, and M. , Tetrahedron Letters, vol.6, pp.4387-4388, 1965.

B. M. Tt and T. Ffffff, J. Journal of the American Chemical Society, vol.95, p.128, 1973.

J. Ttttt, J. Kkkk, S. Iiiiiii, and M. Mmmmmm, Journal of the American Chemical Society, vol.86, p.129, 1964.

A. , K. ;. , W. Mmmmmm, and R. , Tetrahedron Letters, vol.11, p.129, 1970.

J. Ttttt, I. Sssssss, I. Mmm, Y. Oooooo, J. Ttttt et al., The Journal of Organic Chemistry, vol.23, p.131, 1982.

F. Ggggg and Y. ;-m''''', Tetrahedron Letters, vol.22, p.131, 1981.

M. Mmmmm-mmm, J. Rrr, M. Ppp, J. Rrr, and M. Mmmmm-mmm, Tetrahedron Letters, vol.30, issue.00, p.133, 1989.

G. Pppp and C. Ss, Chemtracts -Organic Chemistry, vol.12, p.133, 1999.

B. M. Tt, L. Wwwww, B. M. Tt, T. R. Vvvvvvvvv, B. M. Tt et al., Journal of the American Chemical Society, vol.97, issue.12, pp.81422-81429, 1975.

G. Pppp and C. Ss, Chemtracts -Organic Chemistry, vol.105, p.134, 1983.

K. L. Ggggggg, Journal of the American Chemical Society, vol.114, p.134, 1992.

M. Mmmmm-mmm, L. Mmmmmm, and R. Pppppp, The Journal of Organic Chemistry, vol.63, p.134, 1998.

C. Aaa, J. Aaaa, M. ;. Gggggg, M. Chemistry--a-;-b)-aaa, C. ;. et al., Chemistry -A European Journal, vol.5, pp.615-621, 1999.

A. , N. Aaa, C. ;. , S. Gggggggg, H. Jjj et al., , vol.92, pp.134-138, 2002.

P. , M. Ssssss, L. ;. , M. Ssssss, and L. , Gazz. Chim. Ital, vol.51, p.139, 1921.

B. , L. Rrr, and R. , , vol.65, p.139, 2005.

W. ;. Hhh, E. Uuu, I. Mmmm, R. Uuu, R. C. Mmmm et al., Angewandte Chemie International Edition in English, vol.23, p.139, 1958.

A. W. Hhhhhhh, Justus Liebigs Annalen der Chemie, vol.1867, p.139

J. U. Nnn, Justus Liebigs Annalen der Chemie, vol.1897, p.139

W. P. Wwwww, G. W. Ggggg, and I. K. Uuu, Angewandte Chemie, vol.84, p.139, 1972.

I. Uuu, R. Mmmm, U. Ffffff, and I. Uuu, Angewandte Chemie, vol.71, p.139, 1959.

I. Chemistry, ;. Nnn, V. G. Wiley-vch-verlag-gmbh, &. Co, and . Kgaa, , p.139, 2012.

, Multicomponent Reactions

J. Zzz, H. Bbbb, &. Wiley-vch-verlag-gmbh, . Co, and . Kgaa, , p.139, 2005.

A. Dddddd and I. Uuu, Angewandte Chemie, vol.39, p.139, 2000.

D. Mmmmm, G. Ggggg, P. Hhhhhhhh, I. Uuu, . In-organic et al., , p.141, 1971.

S. ;. Mmmm, S. Uu, M. Mmm, and K. , Angewandte Chemie International Edition, vol.50, p.141, 2011.

C. , N. Rrrrrrr, R. ;. Ee-kkkk, L. Ggggg, L. Ffffff-llll et al., The Journal of Organic Chemistry, vol.77, p.141, 2012.

L. Ee-kkkk, L. Ggggg, J. Oooo, and . Chemie, , vol.44, p.142, 2005.

L. Ee-kkkk, M. Ggggggg, L. Ggggg, E. ;. Mmm-l, A. Ddd-s et al., Organic Letters, vol.8, p.142, 2006.

L. Ee-kkkk, M. Ggggggg, L. Ggggg, and J. Oooo, The Journal of Organic Chemistry, vol.72, p.142, 2007.

M. Ss and D. Ssss, Helvetica Chimica Acta, vol.66, p.142, 1983.

W. , S. , M. , D. Zzz, and J. , Angewandte Chemie International Edition, vol.47, p.142, 2008.

O. , J. M. Pppppp, U. ;. , and B. , Journal of the American Chemical Society, vol.126, p.144, 2004.

E. ;. Mmm-l, L. Ee-kkkk, and L. Ggggg, Tetrahedron Letters, vol.55, p.144, 2014.

A. Ddd-s, L. Ee-kkkk, and . Synlett, , p.145, 1901.

M. Ss, L. Mmmm, and R. Rrr, Advanced Synthesis & Catalysis, vol.358, p.145, 2016.

C. , M. ;. Ddd-s, A. Ee-kkkk, and N. , Chemical Communications, vol.51, p.147, 2015.

E. H. Ee-mmmmmmm, M. ;. ;-c, M. ;. , J. Aaaaaaa, S. Iiiiii et al., Chemical Communications, vol.52, p.147, 2016.

N. , N. ;. Ee-kkkk, and L. , European Journal of Organic Chemistry, vol.166, pp.146-148, 2017.

A. B. Aaaaaa, R. ;. Aaaaaaaaaa, L. Ee-kkkk, and . Synlett, , vol.26, p.150, 2015.

V. V. Gg, H. Aaaaa, C. ;. Aaa, L. Ee-kkkk, L. Ggggg et al., DOI : 10 . 1021 / om00029a052, European Journal of Organic Chemistry, vol.12, p.160, 1993.

. Ll, J. Bbbb, and J. Mmmmm, European Journal of Organic Chemistry, p.178, 2016.

, An apolar Varian VF-1ms (15 m x 0.25 mm internal diameter) capillary column was used. Three methods were used : 1. Injector: T inj 220 ? C; oven: ramp at 15 ? C min ?1 from 85 ? C to 230 ? C then holding at 230 ? C

, Injector: T inj 220 ? C; oven: isothermal at 230 ? C; detector: T det 250 ? C; H 2 flow: 1.0 mL min ?1 . This method has been used for the optimization of the reaction conditions

, Injector: T inj 220 ? C; oven: isothermal at 40 ? C for 3 min then ramp from 40 to 230 ? C at 15 ? C min ?1

, 5-dimethyphenylcarbamate)cellulose grafted on silica, length: 15 cm, = 4,6 mm, particle diameter: 5µm). solution of 79 (63.4 mg, 0.2 mmol, 1 equiv.) in DMF (in a 10 mL microwave suitable vial) were added successively Xantphos (13.9 mg, 24 µmol, 0.12 equiv.) and Pd(dba) 2 (11.5 mg, 20 µmol, 0.1 equiv.). The microwave tube was tightly closed and the reaction mixture was stirred at 80 ? C for 45 min. The solvent was removed under vacuum and the crude residue, Chiral HPLC analysis Chiral HPLC analysis was performed on a Agilent Technologies 1260 infinity apparatus, equiped with a Daicel chiralcel OD-H column (tris, vol.3

, H NMR attribution was performed on enriched fractions

H. Nmr-;-d and J. , 300 MHz, Chloroform-d): ? / ppm 7.32 -7.11 (m, 10H, H Ar ), vol.6

, 6 Hz, 1H, C 3' -H), 6.30 (d, J = 16.0 Hz, 1H, C 3 -H), 5.51 (br d, vol.9

H. Nmr-;-d and J. , 300 MHz, Chloroform-d): ? / ppm 7.32 -7.11 (m, 10H, H Ar ), vol.6

, 10.0 Hz, 1H, C 3' -H), 6.10 (d, J = 16.0 Hz, 1H, C 3 -H), 5.68 (br d, vol.9

, Both pairs (all peaks are split in two and reported here with an interpunct ·

, Chloroform-d): ? / ppm 173.6 · 172.2 (C 5 )

, C Ar ), 128.80 (C Ar ), 128.76 (C Ar ), 128.5 (C Ar ), 127.1 (C Ar ), 127.1 (C Ar ), C Ar ), vol.128, issue.2

, mg, 0.2 mmol, 1 equiv.) in DMF (in a 10 mL microwave suitable vial) were added successively Xantphos (13.9 mg, 24 µmol, 0.12 equiv.) and Pd(dba) 2 (11.5 mg, 20 µmol, 0.1 equiv.). The microwave tube was tightly closed and the reaction mixture was stirred at 80 ? C for 45 min, The solvent was removed under vacuum and the crude residue was purified by flash chromatography on silica gel (PE/AcOEt, vol.90

, H NMR attribution was performed on enriched fractions

H. Nmr, 300 MHz, Chloroform-d): ? / ppm 7.35 -7.20 (m, 10H, H Ar )

H. Nmr, 300 MHz, Chloroform-d): ? / ppm 7.35 -7.20 (m, 10H, H Ar ), vol.7

, 27 (d, J = 16.1 Hz, 1H, C 3 -H), 5.79 (dd, J = 15.3, 1.3 Hz, 1H, C 4, vol.6

, Both pairs (all peaks are split in two and reported here with an interpunct ·

, Chloroform-d): ? / ppm 172

, C 1 and C 1' ), 133.4 · 132.8 (C 2 ), 129.7 (C Ar ), vol.153